TY - JOUR
T1 - IgA-producing lymphoplasmacytic lymphoma carrying the chromosomal abnormality t(8;14)
AU - Gotoh, Yuta
AU - Aoyama, Yumi
AU - Tsunemine, Hiroko
AU - Idei, Yuka
AU - Mori, Ayano
AU - Kodaka, Taiichi
AU - Iba, Sachiko
AU - Tomita, Akihiro
AU - Itoh, Tomoo
AU - Takahashi, Takayuki
N1 - Publisher Copyright:
© 2019 The Japanese Society for Lymphoreticular Tissue Research.
PY - 2019
Y1 - 2019
N2 - IgA-producing lymphoplasmacytic lymphoma (LPL) is rare and IgH/c-myc translocation is rare in LPL. This is the first report of a case of IgA-producing LPL carrying t(8;14). An 86-year-old woman presented inguinal and intra-abdominal lymph node swelling, and lytic bone lesions in the lumbar vertebrae. A diagnosis of IgA-producing LPL was immunohistochemically made by inguinal lymph node biopsy. The serum IgA level was 1,180 mg/dL, which was revealed to be composed of IgA-λ mono-clonal protein. Bone marrow chromosomal analysis demonstrated a complex abnormal karyotype, including t(8;14)(q24;q32), which was confirmed by FISH analysis. Abnormal lymphocytes positive for CD19, CD20, cyIgA, and cyλ were detected on flow cytometry analysis of marrow cells. Best supportive care was selected because of dementia and refractory urinary tract infection. Circulating lymphoplasmacytic cells with the same phenotype and karyotype were observed, and increased in num-ber. The aggressive clinical course, including lytic bone lesions, may have been due to IgH/c-myc translocation or the nature of IgA-producing LPL.
AB - IgA-producing lymphoplasmacytic lymphoma (LPL) is rare and IgH/c-myc translocation is rare in LPL. This is the first report of a case of IgA-producing LPL carrying t(8;14). An 86-year-old woman presented inguinal and intra-abdominal lymph node swelling, and lytic bone lesions in the lumbar vertebrae. A diagnosis of IgA-producing LPL was immunohistochemically made by inguinal lymph node biopsy. The serum IgA level was 1,180 mg/dL, which was revealed to be composed of IgA-λ mono-clonal protein. Bone marrow chromosomal analysis demonstrated a complex abnormal karyotype, including t(8;14)(q24;q32), which was confirmed by FISH analysis. Abnormal lymphocytes positive for CD19, CD20, cyIgA, and cyλ were detected on flow cytometry analysis of marrow cells. Best supportive care was selected because of dementia and refractory urinary tract infection. Circulating lymphoplasmacytic cells with the same phenotype and karyotype were observed, and increased in num-ber. The aggressive clinical course, including lytic bone lesions, may have been due to IgH/c-myc translocation or the nature of IgA-producing LPL.
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U2 - 10.3960/jslrt.19009
DO - 10.3960/jslrt.19009
M3 - Article
AN - SCOPUS:85154588340
SN - 1346-4280
VL - 59
SP - 124
EP - 129
JO - Journal of Clinical and Experimental Hematopathology
JF - Journal of Clinical and Experimental Hematopathology
IS - 3
ER -